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uracil glycol

Known as: 5,6-dihydroxy-5,6-dihydrouracil, Ug cpd 
National Institutes of Health

Papers overview

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2012
2012
Spontaneous and oxidant-induced damage to cytosine is probably the main cause of CG to TA transition mutations in mammalian… Expand
Review
2002
Review
2002
  • S. Wallace
  • Free radical biology & medicine
  • 2002
  • Corpus ID: 11852794
The principal oxidized cytosine bases, uracil glycol, 5-hydroxycytosine, and 5-hydroxyuracil, are readily bypassed, miscode, and… Expand
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Highly Cited
1999
Highly Cited
1999
Saccharomyces cerevisiae possesses two functional homologues (Ntg1p and Ntg2p) of the Escherichia coli endonuclease III protein… Expand
Highly Cited
1998
Highly Cited
1998
A major stable oxidation product of DNA cytosine is uracil glycol (Ug). Because of the potential of Ug to be a strong… Expand
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Highly Cited
1998
Highly Cited
1998
The most common base substitution arising from oxidative damage of DNA is a GC --> AT transition. In an effort to determine the… Expand
Highly Cited
1995
Highly Cited
1995
Exposure of pyrimidines of DNA to ionizing radiation under aerobic conditions or oxidizing agents results in attack on the 5,6… Expand
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Highly Cited
1994
Highly Cited
1994
A variety of chemically modified oligonucleotides have been studied by matrix-assisted laser desorption/ionization time-of-flight… Expand
Highly Cited
1993
Highly Cited
1993
The excision of modified bases from DNA by Escherichia coli endonuclease III was investigated. Modified bases were produced in… Expand
1987
1987
The radiation chemistry of the dinucleoside monophosphate d(CpG) and its sequence isomer, d(GpC), has been examined in aqueous… Expand
Highly Cited
1986
Highly Cited
1986
OsO4 selectively forms thymine glycol lesions in DNA. In the past, OsO4-treated DNA has been used as a substrate in studies of… Expand
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